HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486492Generated: October 30, 2026
Tributylstannane → HCID 178441857, compound
https://huagongshe.com/reaction/486492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178441862 | HCID 178441862 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 178441857 | HCID 178441857 | — |
Reaction Steps
To a solution of 1.0 g of 2-butyl-6-iodo-4(1H)-quinazolinone and 0.355 g of tetrakis(triphenylphosphine)palladium in 15 ml of tetrahydrofuran and 5 ml of N,N-dimethylformamide, heated to 55° C. under an atmosphere of carbon monoxide is added a solution of 1.40 g of tri-n-butyltin hydride in 2.5 ml of toluene over 6 hours via a syringe pump. After the addition is complete the reaction is allowed to cool to room temperature, diluted with brine and extracted with chloroform. The combined organics are concentrated in vacuo and the resulting residue triturated with ether. The precipitate is collected by filtration and purified by flash chromatography on silica gel, eluting with 1:1 ethyl acetate-hexanes to give 0.35 g of the desired product, m.p. 242°-244° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05292734 |
|---|
| Source dataset | uspto-grants-1994_03 |
|---|
| ORD ID | ord-585d6c5062cd41578712e838c3b6d667 |
|---|
| Source note | uspto-grants-1994_03 |
|---|